Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study.
about
Health related quality of life in sickle cell patients: the PiSCES projectAdult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.A video-intervention to improve clinician attitudes toward patients with sickle cell disease: the results of a randomized experimentThe association of provider communication with trust among adults with sickle cell diseaseHospital self-discharge among adults with sickle-cell disease (SCD): associations with trust and interpersonal experiences with care.An unequal burden: poor patient-provider communication and sickle cell disease.Perceived discrimination in health care is associated with a greater burden of pain in sickle cell diseasePerceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell diseaseEvaluation and Treatment of Sickle Cell Pain in the Emergency Department: Paths to a Better FutureHealth care provider attitudes toward patients with acute vaso-occlusive crisis due to sickle cell disease: development of a scale.Health-related stigma in young adults with sickle cell disease.Self-care recommendations of middle-aged and older adults with sickle cell diseaseRespect, trust, and the management of sickle cell disease pain in hospital: comparative analysis of concern-raising behaviors, preliminary model, and agenda for international collaborative research to inform practice.Problematic hospital experiences among adult patients with sickle cell diseaseMore educated emergency department patients are less likely to receive opioids for acute painA Quality Improvement Initiative to Improve Emergency Department Care for Pediatric Patients with Sickle Cell DiseasePsychological complications in sickle cell disease.Emergency department management of acute pain episodes in sickle cell disease.Police officer, deal-maker, or health care provider? Moving to a patient-centered framework for chronic opioid management.The association of optimism and perceived discrimination with health care utilization in adults with sickle cell disease.Care seeking for pain in young adults with sickle cell disease.Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department careSickle Cell Disease: quality of life in patients with hemoglobin SS and SC disordersUtility of WHOQOL-BREF in measuring quality of life in sickle cell diseaseCriterion and convergent validity for 4 measures of pain in a pediatric sickle cell disease population.A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.Barriers to effective pain management in sickle cell disease.Sickle cell disease in the United States: looking back and forward at 100 years of progress in management and survival.An intervention to decrease stigma in young adults with sickle cell disease.Management of the acute painful crisis in sickle cell disease- a re-evaluation of the use of opioids in adult patients.Challenges and resilience in the lives of adults with sickle cell disease.The lives of adults over 30 living with sickle cell disorder.Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial.Cannabis use in sickle cell disease: a questionnaire study.The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease.Treating first episode psychosis--the service users' perspective: a focus group evaluation.Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell DiseaseAdult emergency department patients with sickle cell pain crisis: a learning collaborative model to improve analgesic management.Developing a short form of the simple Rathus assertiveness schedule using a sample of adults with sickle cell disease.Analgesic use and pain coping among patients with haemophilia.
P2860
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P2860
Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Experiences of hospital care a ...... ll disease: qualitative study.
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Experiences of hospital care a ...... ll disease: qualitative study.
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type
label
Experiences of hospital care a ...... ll disease: qualitative study.
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Experiences of hospital care a ...... ll disease: qualitative study.
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Experiences of hospital care a ...... ll disease: qualitative study.
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Experiences of hospital care a ...... ll disease: qualitative study.
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P2093
P2860
P1433
P1476
Experiences of hospital care a ...... ll disease: qualitative study.
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P2093
P2860
P304
P356
10.1136/BMJ.318.7198.1585
P407
P577
1999-06-01T00:00:00Z